Genes of the 1-desoxy -d-xylulose biosynthesis path

ABSTRACT

The invention relates to DNA sequences from  Plasmodium falciparum,  namely the genes lytB and yfgB which, when integrated into the genome of viruses, eukaryotes and prokaryotes, alter the isoprenoid biosynthesis. The invention also relates to gene technological methods for producing these transgenic viruses, eukaryotes and prokaryotes and to methods for identifying substances with a herbicidal, antimicrobial, antiparasitic, antiviral, fungicidal and bactericidal effect in plants and an antimicrobial, antiparasitic, antimycotic, antibacterial and antiviral effect in human beings and animals.

[0001] The present invention relates to DNA sequences which modify isoprenoid synthesis when integrated into the genome of viruses, eukaryotes and prokaryotes and to genetic engineering processes for the production of these transgenic viruses, eukaryotes and prokaryotes. It also relates to methods for the identification of substances having a herbicidal, antimicrobial, antiparasitic, antiviral, fungicidal or bactericidal action in plants or an antimicrobial, antiparasitic, antimycotic, antibacterial or antiviral action in humans and animals.

[0002] The biosynthesis pathway for the formation of isoprenoids via the conventional acetate/mevalonate pathway and an alternative mevalonate-independent biosynthesis pathway, the deoxy-D-xylulose phosphate pathway (DOXP or MEP pathway) are already known (Rohmer, M., Knani, M., Simonin, P., Sutter, B., and Sahm, H. (1993): Biochem. J. 295: 517-524).

[0003] However, how and via what routes a change in the isoprenoid concentration can be achieved via the deoxy-D-xylulose phosphate pathway in viruses, eukaryotes and prokaryotes is not known.

[0004] DNA sequences which code for enzymes which participate in the DOXP pathway are therefore provided. Both genes (lytB and yfgB) and enzymes (LytB and YfgB) participate in isoprenoid biosynthesis and are essential for the survival of the particular organisms (example 1 and 2).

[0005] The invention relates to the following DNA sequences:

[0006] DNA sequences which code for a polypeptide with the amino acid sequence shown in SEQ ID NO: 5 or for an analogue or derivative of the polypeptide according to SEQ ID NO: 5 wherein one or more amino acids have been deleted, added or replaced by other amino acids, without substantially reducing the enzymatic action of the polypeptide, and

[0007] DNA sequences which code for a polypeptide with the amino acid sequence shown in SEQ ID NO: 14 or for an analogue or derivative of the polypeptide according to SEQ ID NO: 14 wherein one or more amino acids have been deleted, added or replaced by other amino acids, without substantially reducing the enzymatic action of the polypeptide.

[0008] The invention is furthermore defined by claims 1 to 4. Further developments of the invention are defined by the sub-claims.

[0009] The genes and their gene products (polypeptides) are listed in the sequence listing with their primary structure and have the following allocation:

[0010] SEQ ID NO: 1: lytB gene

[0011] SEQ ID NO: 5: LytB protein

[0012] SEQ ID NO: 9: yfgB gene

[0013] SEQ ID NO: 14: YfgB protein

[0014] The DNA sequences all originate from Plasmodium falciparum, strain 3D7.

[0015] In addition to the DNA sequences mentioned in the sequence listing, those which have a different DNA sequence as a result of degeneration of the genetic code but code for the same polypeptide or for an analogue or derivative of the polypeptide wherein one or more amino acids have been deleted, added or replaced by other amino acids, without substantially reducing the enzymatic action of the polypeptide, are also suitable.

[0016] The sequences according to the invention are suitable for over-expression of genes in viruses, eukaryotes and prokaryotes which are responsible for isoprenoid biosynthesis of the 1-deoxy-D-xylulose pathway.

[0017] According to the invention, animal cells, plant cells, algae, yeasts and fungi belong to the eukaryotes or eukaryotic cells, and archaebacteria and eubacteria belong to the prokaryotes or prokaryotic cells.

[0018] When a DNA sequence on which one of the abovementioned DNA sequences is located is integrated into a genome, expression of the genes described above in viruses, eukaryotes and prokaryotes becomes possible. The viruses, eukaryotes and prokaryotes transformed according to the invention are cultured in a manner known per se and the isoprenoid formed during this culturing is isolated and optionally purified. Not all the isoprenoids have to be isolated, since in some cases the isoprenoids are released directly into the surrounding air.

[0019] The invention furthermore relates to a process for the production of transgenic viruses, eukaryotes and prokaryotes with isoprenoid expression, which comprises the following steps.

[0020] a) Preparation of a DNA sequence with the following part sequences

[0021] i) promoter which is active in viruses, eukaryotes and prokaryotes and ensures the formation of an RNA in the envisaged target tissue or the target cells,

[0022] ii) DNA sequence which codes for a polypeptide with the amino acid sequence shown in SEQ ID NO: 5 or 14 or for an analogue or derivative of the polypeptide according to SEQ ID NO: 5 or 14,

[0023] iii) 3′-nontranslated sequence which leads to the addition of poly-A radicals on to the 3′-end of the RNA in viruses, eukaryotes and prokaryotes,

[0024] b) transfer and incorporation of the DNA sequence into the genome of viruses or prokaryotic or eukaryotic cells with or without the use of a vector (e.g. plasmid, viral DNA).

[0025] The intact whole plants can be regenerated from the transformed plant cells.

[0026] The sequences with the nucleotide sequences SEQ ID NO: 1 and SEQ ID NO: 9 which code for the proteins can be provided with a promoter which ensures transcription in particular organs or cells and is coupled in the sense orientation (3′-end of the promoter to the 5′-end of the coding sequence) to the sequence which codes the protein to be formed. A termination signal which determines the termination of the mRNA synthesis is attached to the 3′-end of the coding sequence. To direct the protein to be expressed into particular subcellular compartments, such as chloroplasts, amyloplasts, mitochondria, vacuoles, cytosol or intercellular spaces, a sequence which codes for a so-called signal sequence or a transit peptide can also be placed between the promoter and the coding sequence. The sequence must be in the same reading frame as the coding sequence of the protein. For preparation of the introduction of the DNA sequences according to the invention into higher plants, a large number of cloning vectors which comprise a replication signal for E. coli and a marker which allows selection of the transformed cells are available. Examples of vectors are pBR 322, pUC series, M13mp series, pACYC 184, EMBL 3 etc. Further DNA sequences may be required, depending on the method of introduction of desired genes into the plants. For example, if the Ti or Ri plasmid is used for transformation of the plant cells, at least a right limitation, but often the right and the left limitation of the Ti and Ri plasmid T-DNA must be inserted as a flanking region to the genes to be introduced. The use of T-DNA for transformation of plant cells has been investigated intensively and has been described adequately in EP 120516; Hoekama, in: The Binary Plant Vector System, Offset-drukkerij Kanters B. V. Alblasserdam (1985), Chapter V; Fraley et al., Crit.Rev.Plant Sci. 4, 1-46 and An et al. (1985) EMBO J. 4, 277-287. Once the DNA introduced has integrated into the genome, it is as a rule stable and is also retained in the descendants of the cells originally transformed. It usually contains a selection marker, which imparts to the transformed plant cells resistance to a biocide or an antibiotic, such as kanamycin, G 418, bleomycin, hygromycin or phosphinotricin, inter alia. The marker individually used should therefore allow selection of transformed cells over cells in which the DNA inserted is missing.

[0027] Many techniques are available for introduction of DNA into a plant. These techniques include transformation with the aid of agrobacteria, e.g. Agrobacterium tumefaciens, fusion of protoplasts, microinjection of DNA, electroporation, as well as ballistic methods and virus infection. Whole plants can then be regenerated again from the transformed plant material in a suitable medium, which can contain antibiotics or biocides for selection. No specific requirements are imposed on the plasmids for the injection and electroporation. However, if whole plants are to be regenerated from cells transformed in this way, the presence of a selectable marker gene is necessary. The transformed cells grow within the plants in the usual way (McCormick et al. (1986), Plant Cell Reports 5, 81-84). The plants can be grown normally and crossed with plants which have the same transformed genetic disposition or other genetic dispositions. The individuals arising therefrom have the corresponding phenotypic characteristics.

[0028] The invention also provides expression vectors which contain one or more of the DNA sequences according to the invention. Such expression vectors are obtained by providing the DNA sequences according to the invention with suitable functional regulation signals. Such regulation signals are DNA sequences which are responsible for the expression, for example promoters, operators, enhancers and ribosomal binding sites, and are recognized by the host organism.

[0029] Further regulation signals, which control, for example, replication or recombination of the recombinant DNA in the host organism, can optionally also be a constituent of the expression vector.

[0030] The invention also provides the host organisms transformed with the DNA sequences or expression vectors according to the invention.

[0031] Those host cells and organisms which have no intrinsic enzymes of the DOXP pathway are particularly suitable for expression of the enzymes according to the invention. This applies to archaebacteria, animals, some fungi, slime fungi and some eubacteria. The detection and purification of the recombinant enzymes is substantially facilitated by the absence of these intrinsic enzyme activities. It is also possible for the first time, as a result, to measure the activity and in particular the inhibition of the activity of the recombinant enzymes according to the invention by various chemicals and pharmaceuticals in crude extracts from the host cells with a low outlay.

[0032] The expression of the enzymes according to the invention advantageously then takes place in eukaryotic cells if posttranslatory modifications and a natural folding of the polypeptide chain are to be achieved. Depending on the expression system, expression of genomic DNA sequences moreover has the result that introns are eliminated by splicing the DNA and the enzymes are produced in the polypeptide sequence characteristic for the parasites. Sequences which code for introns can also be eliminated from the DNA sequences to be expressed or inserted experimentally by recombinant DNA technology.

[0033] The protein can be isolated from the host cell or the culture supernatant of the host cell by processes known to the expert. In vitro reactivation of the enzymes may also be necessary.

[0034] To facilitate the purification, the enzymes according to the invention or part sequences of the enzymes can be expressed as a fusion protein with various peptide chains. Oligo-histidine sequences and sequences which are derived from glutathione S-transferase, thioredoxin or calmodulin-binding peptides are particularly suitable for this purpose. Fusions with thioredoxin-derived sequences are particularly suitable for prokaryotic expression, since the solubility of the recombinant enzymes is increased as a result.

[0035] The enzymes according to the invention or part sequences of the enzymes can furthermore be expressed as a fusion protein with those peptide chains known to the expert, such that the recombinant enzymes are transported into the extracellular medium or into particular compartments of the host cells. Both the purification and the investigation of the biological activity of the enzymes can be facilitated as a result.

[0036] In the expression of the enzymes according to the invention, it may prove to be expedient to modify individual codons. Targeted replacement of bases in the coding region is also appropriate here if the codons used deviate in the parasites from the codon utilization in the heterologous expression system, in order to ensure optimum synthesis of the protein. Deletions of non-translated 5′- or 3′-sections are furthermore often appropriate, for example if several destabilizing sequence motifs ATTTA are present in the 3′-region of the DNA. These should then be deleted in the case of the preferred expression in eukaryotes. Modifications of this type are deletions, additions or replacement of bases, and the present invention also provides these.

[0037] The enzymes according to the invention can furthermore be obtained by in vitro translation under standardized conditions by techniques known to the expert. Systems which are suitable for this are rabbit reticulocyte and wheat germ extracts and bacterial lysates. Translation of in vitro-transcribed mRNA in Xenopus oocytes is also possible.

[0038] Oligo- and polypeptides with sequences derived from the peptide sequence of the enzymes according to the invention can be prepared by chemical synthesis. With suitable choice of the sequences, such peptides have properties which are characteristic of the complete enzymes according to the invention. Such peptides can be prepared in large amounts and are particularly suitable for studies of the kinetics of the enzyme activity, the regulation of the enzyme activity, the three-dimensional structure of the enzymes, the inhibition of the enzyme activity by various chemicals and pharmaceuticals and the binding geometry and binding affinity of various ligands.

[0039] A DNA with the nucleotides from sequences SEQ ID NO: 1 and 9 is preferably used for recombinant preparation of the enzymes according to the invention.

[0040] As stated above, in addition to the conventional acetate/mevalonate pathway, there is an alternative mevalonate-independent biosynthesis pathway in plants for the formation of isoprenoids, the deoxy-D-xylulose phosphate pathway (DOXP pathway). It has emerged that this deoxy-D-xylulose phosphate metabolic pathway is also present in many parasites, bacteria, viruses and fungi.

[0041] The invention therefore also includes a method for screening a compound. According to this method, a host organism which contains a recombinant expression vector, wherein the vector has at least part of the oligonucleotide sequence according to SEQ ID NO: 1 or SEQ ID NO: 9 or variants or homologues of this, and in addition a compound which is presumed to have an antimicrobial, antiparasitic, antiviral and antimycotic action in humans and animals or a bactericidal, antimicrobial, herbicidal or fungicidal action in plants are provided. The host organism is then brought into contact with the compound and the activity of the compound is determined.

[0042] This invention also provides methods for the determination of the enzymatic activity of the LytB and YfgB protein. This can be determined by the known techniques. In these, the change in the concentration of the intermediates of the DOXP pathway which function as substrates or products of the particular enzymes is determined by photometric, fluorimetric or chromatographic methods. The detection of the change in concentration can also be carried out by coupled enzyme assays, the detection taking place via one or more additional enzymatic steps. The additional enzymes may also participate in the DOXP pathway or can be added experimentally to the system.

EXAMPLE 1

[0043] This investigate whether the lytB gene product is necessary for the survival of the blood stages of the malaria pathogen Plasmodium falciparum, production of a “gene disruption” mutant of P. falciparum was attempted. In this mutant, a gene which codes for a selection marker was to be introduced into the gcpe gene by genetic engineering methods, and this was to be inactivated as a result. For this, a construct (pPflytBKO) which contains an expression cassette which imparts pyrimethamine resistance and is flanked by two fragments from the coding sequence of the lytB gene of P. falciparum was produced. This construct was to be integrated into the gcpe gene by homologous recombination via the flanking sequences.

[0044] All the PCR amplifications described were carried out with heat-stable Pwo DNA polymerase, as a result of which the products acquire smooth ends and are suitable for “blunt end” ligations. The sequence of the lytB gene was amplified with the primers 5′-ATG TCA GTT ACC ACA TTT TGT TCT TTA AAA AAA ACG G-3′ and 5′-GTG ATT TCA TTT TTC TCT TTC TTT TAT CAT C-3′ and genomic DNA from the P. falciparum strain 3D7 as the template, phosphorylated with T4 polynucleotide kinase and cloned into a pUC 19 vector linearized with Sma I (pUCPflytB). The dihydrofolate reductase gene of Toxoplasma gondii (Tg DHFR-TS), which had been modified such that it imparts resistance to pyrimethamine, was used as the selection marker. The expression of TgDHFR-TS took place under the control of the 5′- and 3′-nontranslated elements of the P. falciparum calmodulin (Pf CAM) gene. This expression cassette was obtained from the plasmid pTgD-TS.CAM5/3.KP, which had been constructed according to published protocols (Crabb, B. S. and Cowman, A. F. (1996) Proc. Natl. Acad. Sci. USA, 93, 7289-7294). The expression cassette was obtained by amplification with the primers 5′-AATCTCTGAGCTTCTTCTTTG-3′ and 5′-GGGGGAGCTCGAACTTAATAAAAAAGAGGAG-3′ with pTgD-TS.CAM5/3.KP as the template. The expression cassette was then inserted into the insert of pUCPfgcpe. For this, pUCPflytB was opened with Dsa I in the insert and the overhangs were completed with T4 and Klenow DNA polymerase. The amplified expression cassette was phosphorylated and inserted via “blunt end” ligation, as a result of which pPflytBKO was obtained.

[0045] For transfection by electroporation, the infected erythrocytes (strain 3D7, chiefly ring stages, approx. 15% parasitaemia) of a 10 cm culture dish were pelleted and resuspended in 0.8 ml Cytomix (120 mM KCl; 0.15 mM CaCl₂; 2 mM EGTA; 5 mM MgCl₂; 10 mM K₂HPO₄/KH₂PO₄; 25 mM HEPES, pH 7.6), which contained 150 μg plasmid DNA from pPflytBKO. The electroporation was carried out in 4 mm cells at 2.5 kV, 200 Ohm and 25 μF. The parasites were then plated out again on culture dishes and incubated. 48 h after the transfection 400 nM pyrimethamine was added to the culture medium, and after a further 48 h the pyrimethamine concentration was reduced to 100 nM. After 22 days it was possible to detect resistant parasites under the microscope. After 6 weeks the pyrimethamine concentration was increased to 2 μM for a further 3 weeks. The parasites were cloned by limiting dilution on 96-well cell culture plates and cultured for 11 days in the absence of pyrimethamine. 1 μM pyrimethamine was then added again. Episomal plasmids are lost by culture in the absence of pyrimethamine, and during the subsequent renewed selection only parasites which have integrated the plasmid chromosomally can survive.

[0046] Parasites grew in only 5 wells, since the plasmid evidently was present episomally in most of the parasites. It was still possible to detect expression of the lytB gene by RT-PCR in these clones. The plasmid was thus integrated into the genome by non-homologous recombination and the lytB gene of the parasites was not inactivated. Parasites with an inactivated lytB gene are thus evidently not viable, and the gene is therefore essential. According to recent findings, the genus Plasmodium is phylogenetically close to lower algae (Fichera, M. E. and Roos, D. S. (1997) Nature, 390, 407-409; Köhler, S, Delwiche, C. F., Denny, P. W., Tilney, L. G., Webster, P., Wilson, R. J. M., Palmer, J. D. and Roos, D. S. (1997) Nature, 275, 1485-1489). It is therefore to be deduced that the lytB gene is evidently also essential for plants.

EXAMPLE 2

[0047] To investigate whether the yfgB gene product is necessary for the survival of the blood stages of the malaria pathogen Plasmodium falciparum, production of a “gene disruption” mutant of P. falciparum was attempted. In this mutant, a gene which codes for a selection marker was to be introduced into the yfgB gene by genetic engineering methods, and this was to be inactivated as a result. For this, a construct (pPfyfgBKO) which contains an expression cassette which imparts pyrimethamine resistance and is flanked by two fragments from the coding sequence of the yfgB gene of P. falciparum was produced. This construct was to be integrated into the gcpe gene by homologous recombination via the flanking sequences.

[0048] All the PCR amplifications described were carried out with heat-stable Pwo DNA polymerase, as a result of which the products acquire smooth ends and are suitable for “blunt end” ligations. The yfgB sequence was amplified with the primers 5′-ATG GAA AAG TCA AAA AGG TAC ATA AGC CTG-3′ and 5′-AGC ATC GTC CAA ACG ATG AAA ATT TTC GTC-3′ and genomic DNA from the P. falciparum strain 3D7 as the template, phosphorylated with T4 polynucleotide kinase and cloned into a pUC 19 vector linearized with Sma I (pUCPfyfgB). The dihydrofolate reductase gene of Toxoplasma gondii (Tg DHFR-TS), which had been modified such that it imparts resistance to pyrimethamine, was used as the selection marker. The expression of TgDHFR-TS took place under the control of the 5′- and 3′-nontranslated elements of the P. falciparum calmodulin (Pf CAM) gene. This expression cassette was obtained from the plasmid pTgD-TS.CAM5/3.KP, which had been constructed according to published protocols (Crabb, B. S. and Cowman, A. F. (1996) Proc. Natl. Acad. Sci. USA, 93, 7289-7294). The expression cassette was obtained by amplification with the primers 5′-AATCTCTGAGCTTCTTCTTTG-3′ and 5′-GGGGGAGCTCGAACTTAATAAAAAAGAGGAG-3′ with pTgD-TS.CAM5/3.KP as the template. The expression cassette was then inserted into the insert of pUCPfyfgB. For this, pUCPfgcpe was opened with Pac I in the insert and the overhangs were completed with T4 and Klenow DNA polymerase. The amplified expression cassette was phosphorylated and inserted via “blunt end” ligation, as a result of which pPfyfgBKO was obtained.

[0049] For transfection by electroporation, the infected erythrocytes (strain 3D7, chiefly ring stages, approx. 15% parasitaemia) of a 10 cm culture dish were pelleted and resuspended in 0.8 ml Cytomix (120 mM KC1; 0.15 mM CaCl₂; 2 mM EGTA; 5 mM MgCl₂; 10 mM K₂HPO₄/KH₂PO₄; 25 mM HEPES, pH 7.6), which contained 150 μg plasmid DNA from pPfyfgBKO. The electroporation was carried out in 4 mm cells at 2.5 kV, 200 Ohm and 25 μF. The parasites were then plated out again on culture dishes and incubated. 48 h after the transfection 400 nM pyrimethamine was added to the culture medium, and after a further 48 h the pyrimethamine concentration was reduced to 100 nM. After 18 days it was possible to detect resistant parasites under the microscope. After 6 weeks the pyrimethamine concentration was increased to 2 μM for a further 3 weeks. The parasites were cloned by limiting dilution on 96-well cell culture plates and cultured for 11 days in the absence of pyrimethamine. 1 μM pyrimethamine was then added again. Episomal plasmids are lost by culture in the absence of pyrimethamine, and during the subsequent renewed selection only parasites which have integrated the plasmid chromosomally can survive. None of the parasite clones survived the renewed addition of pyrimethamine. This result indicates that parasites with an inactivated yfgB gene are not viable, and the gene is therefore essential. According to recent findings, the genus Plasmodium is phylogenetically close to lower algae (Fichera, M. E. and Roos, D. S. (1997) Nature, 390, 407-409; Köhler, S, Delwiche, C. F., Denny, P. W., Tilney, L. G., Webster, P., Wilson, R. J. M., Palmer, J. D. and Roos, D. S. (1997) Nature, 275, 1485-1489). It is therefore to be deduced that the yfgB gene is evidently also essential for plants.

EXAMPLE 3 The yfgB is Essential for Escherichia Coli

[0050] Construction of the gene replacement plasmid pKO3-ΔyfgB

[0051] The pKO3 vector was used to produce a deletion mutant of E. coli (Link, A. J.; Phillips, D.; Church, G. M.; J. Bacteriol. 179, 6228-6237). To produce the deletion construct, two sequences downstream and upstream of the yfgB gene were amplified in two asymmetric PCR batches. The primers were employed in a 1:10 molar ratio (50 nM and 500 nM). The two PCR products were fused to one product in a second PCR amplification. The product was cloned using the pCR-TA-TOPO Cloning Kit (Invitrogen) and cloned into the pKO3 vector via the restriction cleavage sites Bam HI and Sal I. The following primers were used: yfgB-N-out, 5′-AGGATCCtccatcatcaaaccgaac-3′ yfgB-N-in, 5′-TCCCATCCACTAAACTTAAACATctattccggcctcgttat-3′ yfgB-C-in, 5′-ATGTTTAAGTTTAGTGGATGGGaagcggtctgatagccatt-3′ yfgB-C-out, 5′-AGTCGACaagtggagcctgcttttc-3′.

[0052] The restriction cleavage sites are underlined. Overlapping sequences which define a 21 bp “in frame” insertion are printed in bold.

[0053] Construction of the Deletion Mutant wtΔyfgB

[0054] The “gene replacement” experiments were carried out in a manner similar to that described (Link, A. J.; Phillips, D.; Church, G. M.; J. Bacteriol. 179, 6228-6237). The plasmid pKO3-ΔyfgB was transformed into the E. coli K-12 strain DSM No. 498 (ATCC 23716). After incubation for 1 h at 30° C., bacteria with integrated plasmid were selected by a temperature shift to 43° C. By subsequent testing for sucrose resistance and chloramphenicol sensitivity, bacteria which had lost the vector sequences were selected and then analysed for the desired genotype by PCR. No bacteria with a yfgB deletion were to be discovered, which demonstrates that the yfgB gene is essential for E. coli.

1 28 1 1920 DNA Plasmodium falciparum CDS (1)..(1920) 1 tta tac aca tat tga aca aaa aaa aaa aag aaa aaa aaa aaa aaa aaa 48 Leu Tyr Thr Tyr Thr Lys Lys Lys Lys Lys Lys Lys Lys Lys Lys 1 5 10 15 aaa aaa aaa aaa cta tta act tat att ttt tat gta tta tta tat tat 96 Lys Lys Lys Lys Leu Leu Thr Tyr Ile Phe Tyr Val Leu Leu Tyr Tyr 20 25 30 cta tac ttt cat tta ttt att tat tta ttt tat ttt att ttt ttt att 144 Leu Tyr Phe His Leu Phe Ile Tyr Leu Phe Tyr Phe Ile Phe Phe Ile 35 40 45 tcc cga taa cgt tat ata tat tta tat ata tat ata tat ata taa tat 192 Ser Arg Arg Tyr Ile Tyr Leu Tyr Ile Tyr Ile Tyr Ile Tyr 50 55 60 ata att aat atg tca gtt acc aca ttt tgt tct tta aaa aaa acg gac 240 Ile Ile Asn Met Ser Val Thr Thr Phe Cys Ser Leu Lys Lys Thr Asp 65 70 75 aag tgc aat att tat att tca aaa agg gct ttc tct gtg ttt tta ttt 288 Lys Cys Asn Ile Tyr Ile Ser Lys Arg Ala Phe Ser Val Phe Leu Phe 80 85 90 tat ttg ttt ttt ttt tta ttc ttc cat ttt tat ttt cta tgt tct tca 336 Tyr Leu Phe Phe Phe Leu Phe Phe His Phe Tyr Phe Leu Cys Ser Ser 95 100 105 tca ttt gct gtt atc ata cat gaa agt gaa aaa agg aaa aat atc atg 384 Ser Phe Ala Val Ile Ile His Glu Ser Glu Lys Arg Lys Asn Ile Met 110 115 120 125 aga agg aaa aga tca ata cta caa ata ttt gaa aat tct ata aaa tcc 432 Arg Arg Lys Arg Ser Ile Leu Gln Ile Phe Glu Asn Ser Ile Lys Ser 130 135 140 aaa gaa gga aaa tgt aat ttt aca aaa aga tat ata act cat tat tat 480 Lys Glu Gly Lys Cys Asn Phe Thr Lys Arg Tyr Ile Thr His Tyr Tyr 145 150 155 aat atc cca tta aaa atc aaa aaa cat gac tta ccc agt gtt ata aaa 528 Asn Ile Pro Leu Lys Ile Lys Lys His Asp Leu Pro Ser Val Ile Lys 160 165 170 tat ttt tct cat aaa cct aat gga aag cat aat tat gtt aca aat atg 576 Tyr Phe Ser His Lys Pro Asn Gly Lys His Asn Tyr Val Thr Asn Met 175 180 185 att aca caa aag aat aga aaa tcg ttt cta ttt ttt ttt ttc cta tat 624 Ile Thr Gln Lys Asn Arg Lys Ser Phe Leu Phe Phe Phe Phe Leu Tyr 190 195 200 205 aat aag tat ttc ttc gga aaa caa gaa cag ata aga aaa atg aat tat 672 Asn Lys Tyr Phe Phe Gly Lys Gln Glu Gln Ile Arg Lys Met Asn Tyr 210 215 220 cat gaa gaa atg aat aaa ata aat ata aaa aat gat ggg aat cga aaa 720 His Glu Glu Met Asn Lys Ile Asn Ile Lys Asn Asp Gly Asn Arg Lys 225 230 235 ata tat atg tac cca aaa aat gac att cat gaa gag gat ggt gat cat 768 Ile Tyr Met Tyr Pro Lys Asn Asp Ile His Glu Glu Asp Gly Asp His 240 245 250 aag aat gat gtc gaa ata aat caa aaa agg aat gaa caa aat tgt aaa 816 Lys Asn Asp Val Glu Ile Asn Gln Lys Arg Asn Glu Gln Asn Cys Lys 255 260 265 tcg ttt aat gat gaa aaa aac gaa aat gct aga gat cca aac aaa ata 864 Ser Phe Asn Asp Glu Lys Asn Glu Asn Ala Arg Asp Pro Asn Lys Ile 270 275 280 285 tta tat ttg att aac ccc cgt ggt ttt tgc aaa ggt gtt agt cgg gct 912 Leu Tyr Leu Ile Asn Pro Arg Gly Phe Cys Lys Gly Val Ser Arg Ala 290 295 300 ata gaa acg gta gaa gag tgc tta aaa tta ttt aaa cca cct ata tat 960 Ile Glu Thr Val Glu Glu Cys Leu Lys Leu Phe Lys Pro Pro Ile Tyr 305 310 315 gta aaa cac aaa ata gtt cat aac gat att gtt tgt aaa aaa tta gag 1008 Val Lys His Lys Ile Val His Asn Asp Ile Val Cys Lys Lys Leu Glu 320 325 330 aaa gaa gga gca ata ttt att gaa gat tta aat gac gta cct gat gga 1056 Lys Glu Gly Ala Ile Phe Ile Glu Asp Leu Asn Asp Val Pro Asp Gly 335 340 345 cat ata tta att tat tca gca cat ggt att agt cct caa ata cga gaa 1104 His Ile Leu Ile Tyr Ser Ala His Gly Ile Ser Pro Gln Ile Arg Glu 350 355 360 365 ata gca aaa aaa aaa aaa tta ata gaa ata gat gct aca tgc cct tta 1152 Ile Ala Lys Lys Lys Lys Leu Ile Glu Ile Asp Ala Thr Cys Pro Leu 370 375 380 gtt aat aaa gta cat gta tat gta caa atg aaa gca aaa gaa aat tat 1200 Val Asn Lys Val His Val Tyr Val Gln Met Lys Ala Lys Glu Asn Tyr 385 390 395 gac att att ctt ata gga tat aaa aat cat gta gag gtt ata ggt acc 1248 Asp Ile Ile Leu Ile Gly Tyr Lys Asn His Val Glu Val Ile Gly Thr 400 405 410 tat aat gaa gca cca cat tgt aca cat att gtg gaa aat gtt aat gat 1296 Tyr Asn Glu Ala Pro His Cys Thr His Ile Val Glu Asn Val Asn Asp 415 420 425 gta gat aaa tta aat ttc cca tta aat aaa aag tta ttc tat gtt aca 1344 Val Asp Lys Leu Asn Phe Pro Leu Asn Lys Lys Leu Phe Tyr Val Thr 430 435 440 445 caa acc aca cta agt atg gat gat tgt gca ctt atc gta caa aaa ctc 1392 Gln Thr Thr Leu Ser Met Asp Asp Cys Ala Leu Ile Val Gln Lys Leu 450 455 460 aaa aat aaa ttc cca cat att gaa act ata cct agt gga tcc ata tgt 1440 Lys Asn Lys Phe Pro His Ile Glu Thr Ile Pro Ser Gly Ser Ile Cys 465 470 475 tat gct act aca aat aga caa acg gct ctt aat aaa ata tgt aca aaa 1488 Tyr Ala Thr Thr Asn Arg Gln Thr Ala Leu Asn Lys Ile Cys Thr Lys 480 485 490 tgt gat ctt acc ata gtt gtt ggt agt tct tca tct tct aat gcc aaa 1536 Cys Asp Leu Thr Ile Val Val Gly Ser Ser Ser Ser Ser Asn Ala Lys 495 500 505 aaa tta gtc tat tca tcc caa atc aga aat gtt cca gca gta tta ctt 1584 Lys Leu Val Tyr Ser Ser Gln Ile Arg Asn Val Pro Ala Val Leu Leu 510 515 520 525 aat aca gta cat gat tta gat caa caa ata ctt aag aat gtt aat aaa 1632 Asn Thr Val His Asp Leu Asp Gln Gln Ile Leu Lys Asn Val Asn Lys 530 535 540 ata gca cta act tct gct gcc tca acc cca gag caa gaa aca caa aaa 1680 Ile Ala Leu Thr Ser Ala Ala Ser Thr Pro Glu Gln Glu Thr Gln Lys 545 550 555 ttt gtc aac cta tta aca aac cct cca ttt aat tat acc tta caa aat 1728 Phe Val Asn Leu Leu Thr Asn Pro Pro Phe Asn Tyr Thr Leu Gln Asn 560 565 570 ttt gac ggg gct cac gaa aat gtg ccc aaa tgg aag ctt ccc aag aat 1776 Phe Asp Gly Ala His Glu Asn Val Pro Lys Trp Lys Leu Pro Lys Asn 575 580 585 ttc ttg cac atg ata aaa gaa aga gaa aaa tga aat cac aaa aaa aaa 1824 Phe Leu His Met Ile Lys Glu Arg Glu Lys Asn His Lys Lys Lys 590 595 600 aaa aaa tat ata tat ata tat ata tat ata tat ata tat ata taa ata 1872 Lys Lys Tyr Ile Tyr Ile Tyr Ile Tyr Ile Tyr Ile Tyr Ile Ile 605 610 615 aat tag tga aaa aaa aaa aat ttt ttt tta cat ttt gca cac aat tta 1920 Asn Lys Lys Lys Asn Phe Phe Leu His Phe Ala His Asn Leu 620 625 630 2 4 PRT Plasmodium falciparum 2 Leu Tyr Thr Tyr 1 3 45 PRT Plasmodium falciparum 3 Thr Lys Lys Lys Lys Lys Lys Lys Lys Lys Lys Lys Lys Lys Lys Leu 1 5 10 15 Leu Thr Tyr Ile Phe Tyr Val Leu Leu Tyr Tyr Leu Tyr Phe His Leu 20 25 30 Phe Ile Tyr Leu Phe Tyr Phe Ile Phe Phe Ile Ser Arg 35 40 45 4 11 PRT Plasmodium falciparum 4 Arg Tyr Ile Tyr Leu Tyr Ile Tyr Ile Tyr Ile 1 5 10 5 539 PRT Plasmodium falciparum 5 Tyr Ile Ile Asn Met Ser Val Thr Thr Phe Cys Ser Leu Lys Lys Thr 1 5 10 15 Asp Lys Cys Asn Ile Tyr Ile Ser Lys Arg Ala Phe Ser Val Phe Leu 20 25 30 Phe Tyr Leu Phe Phe Phe Leu Phe Phe His Phe Tyr Phe Leu Cys Ser 35 40 45 Ser Ser Phe Ala Val Ile Ile His Glu Ser Glu Lys Arg Lys Asn Ile 50 55 60 Met Arg Arg Lys Arg Ser Ile Leu Gln Ile Phe Glu Asn Ser Ile Lys 65 70 75 80 Ser Lys Glu Gly Lys Cys Asn Phe Thr Lys Arg Tyr Ile Thr His Tyr 85 90 95 Tyr Asn Ile Pro Leu Lys Ile Lys Lys His Asp Leu Pro Ser Val Ile 100 105 110 Lys Tyr Phe Ser His Lys Pro Asn Gly Lys His Asn Tyr Val Thr Asn 115 120 125 Met Ile Thr Gln Lys Asn Arg Lys Ser Phe Leu Phe Phe Phe Phe Leu 130 135 140 Tyr Asn Lys Tyr Phe Phe Gly Lys Gln Glu Gln Ile Arg Lys Met Asn 145 150 155 160 Tyr His Glu Glu Met Asn Lys Ile Asn Ile Lys Asn Asp Gly Asn Arg 165 170 175 Lys Ile Tyr Met Tyr Pro Lys Asn Asp Ile His Glu Glu Asp Gly Asp 180 185 190 His Lys Asn Asp Val Glu Ile Asn Gln Lys Arg Asn Glu Gln Asn Cys 195 200 205 Lys Ser Phe Asn Asp Glu Lys Asn Glu Asn Ala Arg Asp Pro Asn Lys 210 215 220 Ile Leu Tyr Leu Ile Asn Pro Arg Gly Phe Cys Lys Gly Val Ser Arg 225 230 235 240 Ala Ile Glu Thr Val Glu Glu Cys Leu Lys Leu Phe Lys Pro Pro Ile 245 250 255 Tyr Val Lys His Lys Ile Val His Asn Asp Ile Val Cys Lys Lys Leu 260 265 270 Glu Lys Glu Gly Ala Ile Phe Ile Glu Asp Leu Asn Asp Val Pro Asp 275 280 285 Gly His Ile Leu Ile Tyr Ser Ala His Gly Ile Ser Pro Gln Ile Arg 290 295 300 Glu Ile Ala Lys Lys Lys Lys Leu Ile Glu Ile Asp Ala Thr Cys Pro 305 310 315 320 Leu Val Asn Lys Val His Val Tyr Val Gln Met Lys Ala Lys Glu Asn 325 330 335 Tyr Asp Ile Ile Leu Ile Gly Tyr Lys Asn His Val Glu Val Ile Gly 340 345 350 Thr Tyr Asn Glu Ala Pro His Cys Thr His Ile Val Glu Asn Val Asn 355 360 365 Asp Val Asp Lys Leu Asn Phe Pro Leu Asn Lys Lys Leu Phe Tyr Val 370 375 380 Thr Gln Thr Thr Leu Ser Met Asp Asp Cys Ala Leu Ile Val Gln Lys 385 390 395 400 Leu Lys Asn Lys Phe Pro His Ile Glu Thr Ile Pro Ser Gly Ser Ile 405 410 415 Cys Tyr Ala Thr Thr Asn Arg Gln Thr Ala Leu Asn Lys Ile Cys Thr 420 425 430 Lys Cys Asp Leu Thr Ile Val Val Gly Ser Ser Ser Ser Ser Asn Ala 435 440 445 Lys Lys Leu Val Tyr Ser Ser Gln Ile Arg Asn Val Pro Ala Val Leu 450 455 460 Leu Asn Thr Val His Asp Leu Asp Gln Gln Ile Leu Lys Asn Val Asn 465 470 475 480 Lys Ile Ala Leu Thr Ser Ala Ala Ser Thr Pro Glu Gln Glu Thr Gln 485 490 495 Lys Phe Val Asn Leu Leu Thr Asn Pro Pro Phe Asn Tyr Thr Leu Gln 500 505 510 Asn Phe Asp Gly Ala His Glu Asn Val Pro Lys Trp Lys Leu Pro Lys 515 520 525 Asn Phe Leu His Met Ile Lys Glu Arg Glu Lys 530 535 6 19 PRT Plasmodium falciparum 6 Asn His Lys Lys Lys Lys Lys Tyr Ile Tyr Ile Tyr Ile Tyr Ile Tyr 1 5 10 15 Ile Tyr Ile 7 13 PRT Plasmodium falciparum 7 Lys Lys Lys Asn Phe Phe Leu His Phe Ala His Asn Leu 1 5 10 8 2 PRT Plasmodium falciparum 8 Ile Asn 1 9 1320 DNA Plasmodium falciparum gene (1)..(1320) 9 taa ata aat aaa tta taa atc ttt caa gaa tat att ttt tat aaa aac 48 Ile Asn Lys Leu Ile Phe Gln Glu Tyr Ile Phe Tyr Lys Asn 1 5 10 ata aaa tat aaa ata tac ata tat ata tat ata tat att tta tat tac 96 Ile Lys Tyr Lys Ile Tyr Ile Tyr Ile Tyr Ile Tyr Ile Leu Tyr Tyr 15 20 25 30 ttt taa aat tat tta ttt ata caa atg gaa att taa tgt gaa gaa tag 144 Phe Asn Tyr Leu Phe Ile Gln Met Glu Ile Cys Glu Glu 35 40 aaa aaa cat ttt gtc aat atg gaa aag tca aaa agg tac ata agc ctg 192 Lys Lys His Phe Val Asn Met Glu Lys Ser Lys Arg Tyr Ile Ser Leu 45 50 55 att aag atg atg gaa agg aaa aaa ttt gag aag tat aga tta aaa caa 240 Ile Lys Met Met Glu Arg Lys Lys Phe Glu Lys Tyr Arg Leu Lys Gln 60 65 70 75 ata atg gat aat ata tat aaa gga aaa ata att gaa ata aat aaa atg 288 Ile Met Asp Asn Ile Tyr Lys Gly Lys Ile Ile Glu Ile Asn Lys Met 80 85 90 aaa aat att cca act gaa ata aga aga gaa tta aaa aat ata ttt cat 336 Lys Asn Ile Pro Thr Glu Ile Arg Arg Glu Leu Lys Asn Ile Phe His 95 100 105 aat aat att tta agt ata aaa ccg atc aaa gaa tta aaa tat gat aga 384 Asn Asn Ile Leu Ser Ile Lys Pro Ile Lys Glu Leu Lys Tyr Asp Arg 110 115 120 gca tat aaa gta tta ttt cag tgt aaa gat aat gaa aag att gaa gca 432 Ala Tyr Lys Val Leu Phe Gln Cys Lys Asp Asn Glu Lys Ile Glu Ala 125 130 135 aca tca tta gat ttt ggt tcg cat aaa tct tta tgt ata tct agc caa 480 Thr Ser Leu Asp Phe Gly Ser His Lys Ser Leu Cys Ile Ser Ser Gln 140 145 150 155 ata ggt tgt tct ttt gga tgt aag ttt tgt gct act ggt caa att ggt 528 Ile Gly Cys Ser Phe Gly Cys Lys Phe Cys Ala Thr Gly Gln Ile Gly 160 165 170 ata aaa aga caa tta gat ata gat gaa ata act gat caa ctt tta tat 576 Ile Lys Arg Gln Leu Asp Ile Asp Glu Ile Thr Asp Gln Leu Leu Tyr 175 180 185 ttt caa tca aaa gga gtt gat ata aaa aat ata tct ttt atg ggt atg 624 Phe Gln Ser Lys Gly Val Asp Ile Lys Asn Ile Ser Phe Met Gly Met 190 195 200 gga gaa cct tta gct aat cca tat gtt ttt gat tct ata caa ttt ttt 672 Gly Glu Pro Leu Ala Asn Pro Tyr Val Phe Asp Ser Ile Gln Phe Phe 205 210 215 aat gat aat aat tta ttt tct ata tct aat aga cgt att aat ata tct 720 Asn Asp Asn Asn Leu Phe Ser Ile Ser Asn Arg Arg Ile Asn Ile Ser 220 225 230 235 act gtt ggt ctt tta cca gga att aaa aaa tta aat aac atc ttt cct 768 Thr Val Gly Leu Leu Pro Gly Ile Lys Lys Leu Asn Asn Ile Phe Pro 240 245 250 caa gtt aat tta gct ttc tca tta cat tct cca ttt act gaa gaa agg 816 Gln Val Asn Leu Ala Phe Ser Leu His Ser Pro Phe Thr Glu Glu Arg 255 260 265 gat caa ctt gta cca att aat aaa ttg ttt ccg ttt aat gaa gtt ttt 864 Asp Gln Leu Val Pro Ile Asn Lys Leu Phe Pro Phe Asn Glu Val Phe 270 275 280 gat tta tta gat gaa aga ata gca aaa act ggt aga aga gtt tgg ata 912 Asp Leu Leu Asp Glu Arg Ile Ala Lys Thr Gly Arg Arg Val Trp Ile 285 290 295 agt tat att tta att aaa aat ctt aat gac tcc aaa gat cat gca gaa 960 Ser Tyr Ile Leu Ile Lys Asn Leu Asn Asp Ser Lys Asp His Ala Glu 300 305 310 315 gct ttg tct gat cat ata tgt aaa aga cca aat aac ata aga tac tta 1008 Ala Leu Ser Asp His Ile Cys Lys Arg Pro Asn Asn Ile Arg Tyr Leu 320 325 330 tat aat gta tgt tta ata cct tat aat aaa ggt aat aga att tat aat 1056 Tyr Asn Val Cys Leu Ile Pro Tyr Asn Lys Gly Asn Arg Ile Tyr Asn 335 340 345 ata tca ttt gaa tat ata tat ata tat ata tat tta cta ata ata aaa 1104 Ile Ser Phe Glu Tyr Ile Tyr Ile Tyr Ile Tyr Leu Leu Ile Ile Lys 350 355 360 aaa aag ata tta tgt aaa tat att atg ttt cac aca tta tat aaa tat 1152 Lys Lys Ile Leu Cys Lys Tyr Ile Met Phe His Thr Leu Tyr Lys Tyr 365 370 375 ata ggc ata gag gac atg tta taa aaa agt gca aca tat ata tat ata 1200 Ile Gly Ile Glu Asp Met Leu Lys Ser Ala Thr Tyr Ile Tyr Ile 380 385 390 tat ata tat ata tat ata tat ata cat ttt ttt tat att tat att atc 1248 Tyr Ile Tyr Ile Tyr Ile Tyr Ile His Phe Phe Tyr Ile Tyr Ile Ile 395 400 405 410 ttt tta ata cat tta ttc cat tac att gca gcc aaa aat gtt gac gaa 1296 Phe Leu Ile His Leu Phe His Tyr Ile Ala Ala Lys Asn Val Asp Glu 415 420 425 aat ttt cat cgt ttg gac gat gct 1320 Asn Phe His Arg Leu Asp Asp Ala 430 10 4 PRT Plasmodium falciparum 10 Ile Asn Lys Leu 1 11 27 PRT Plasmodium falciparum 11 Ile Phe Gln Glu Tyr Ile Phe Tyr Lys Asn Ile Lys Tyr Lys Ile Tyr 1 5 10 15 Ile Tyr Ile Tyr Ile Tyr Ile Leu Tyr Tyr Phe 20 25 12 9 PRT Plasmodium falciparum 12 Asn Tyr Leu Phe Ile Gln Met Glu Ile 1 5 13 343 PRT Plasmodium falciparum 13 Lys Lys His Phe Val Asn Met Glu Lys Ser Lys Arg Tyr Ile Ser Leu 1 5 10 15 Ile Lys Met Met Glu Arg Lys Lys Phe Glu Lys Tyr Arg Leu Lys Gln 20 25 30 Ile Met Asp Asn Ile Tyr Lys Gly Lys Ile Ile Glu Ile Asn Lys Met 35 40 45 Lys Asn Ile Pro Thr Glu Ile Arg Arg Glu Leu Lys Asn Ile Phe His 50 55 60 Asn Asn Ile Leu Ser Ile Lys Pro Ile Lys Glu Leu Lys Tyr Asp Arg 65 70 75 80 Ala Tyr Lys Val Leu Phe Gln Cys Lys Asp Asn Glu Lys Ile Glu Ala 85 90 95 Thr Ser Leu Asp Phe Gly Ser His Lys Ser Leu Cys Ile Ser Ser Gln 100 105 110 Ile Gly Cys Ser Phe Gly Cys Lys Phe Cys Ala Thr Gly Gln Ile Gly 115 120 125 Ile Lys Arg Gln Leu Asp Ile Asp Glu Ile Thr Asp Gln Leu Leu Tyr 130 135 140 Phe Gln Ser Lys Gly Val Asp Ile Lys Asn Ile Ser Phe Met Gly Met 145 150 155 160 Gly Glu Pro Leu Ala Asn Pro Tyr Val Phe Asp Ser Ile Gln Phe Phe 165 170 175 Asn Asp Asn Asn Leu Phe Ser Ile Ser Asn Arg Arg Ile Asn Ile Ser 180 185 190 Thr Val Gly Leu Leu Pro Gly Ile Lys Lys Leu Asn Asn Ile Phe Pro 195 200 205 Gln Val Asn Leu Ala Phe Ser Leu His Ser Pro Phe Thr Glu Glu Arg 210 215 220 Asp Gln Leu Val Pro Ile Asn Lys Leu Phe Pro Phe Asn Glu Val Phe 225 230 235 240 Asp Leu Leu Asp Glu Arg Ile Ala Lys Thr Gly Arg Arg Val Trp Ile 245 250 255 Ser Tyr Ile Leu Ile Lys Asn Leu Asn Asp Ser Lys Asp His Ala Glu 260 265 270 Ala Leu Ser Asp His Ile Cys Lys Arg Pro Asn Asn Ile Arg Tyr Leu 275 280 285 Tyr Asn Val Cys Leu Ile Pro Tyr Asn Lys Gly Asn Arg Ile Tyr Asn 290 295 300 Ile Ser Phe Glu Tyr Ile Tyr Ile Tyr Ile Tyr Leu Leu Ile Ile Lys 305 310 315 320 Lys Lys Ile Leu Cys Lys Tyr Ile Met Phe His Thr Leu Tyr Lys Tyr 325 330 335 Ile Gly Ile Glu Asp Met Leu 340 14 48 PRT Plasmodium falciparum 14 Lys Ser Ala Thr Tyr Ile Tyr Ile Tyr Ile Tyr Ile Tyr Ile Tyr Ile 1 5 10 15 His Phe Phe Tyr Ile Tyr Ile Ile Phe Leu Ile His Leu Phe His Tyr 20 25 30 Ile Ala Ala Lys Asn Val Asp Glu Asn Phe His Arg Leu Asp Asp Ala 35 40 45 15 3 PRT Plasmodium falciparum 15 Cys Glu Glu 1 16 5 DNA Plasmodium falciparum 16 attta 5 17 37 DNA Plasmodium falciparum 17 atgtcagtta ccacattttg ttctttaaaa aaaacgg 37 18 31 DNA Plasmodium falciparum 18 gtgatttcat ttttctcttt cttttatcat c 31 19 21 DNA Plasmodium falciparum 19 aatctctgag cttcttcttt g 21 20 31 DNA Plasmodium falciparum 20 gggggagctc gaacttaata aaaaagagga g 31 21 30 DNA Plasmodium falciparum 21 atggaaaagt caaaaaggta cataagcctg 30 22 30 DNA Plasmodium falciparum 22 agcatcgtcc aaacgatgaa aattttcgtc 30 23 21 DNA Plasmodium falciparum 23 aatctctgag cttcttcttt g 21 24 31 DNA Plasmodium falciparum 24 gggggagctc gaacttaata aaaaagagga g 31 25 25 DNA Plasmodium falciparum 25 aggatcctcc atcatcaaac cgaac 25 26 41 DNA Plasmodium falciparum 26 tcccatccac taaacttaaa catctattcc ggcctcgtta t 41 27 41 DNA Plasmodium falciparum 27 atgtttaagt ttagtggatg ggaagcggtc tgatagccat t 41 28 25 DNA Plasmodium falciparum 28 agtcgacaag tggagcctgc ttttc 25 

1. DNA sequences which code for a polypeptide with the amino acid sequence shown in SEQ ID NO: 5 or for an analogue or derivative of the polypeptide according to SEQ ID NO: 5 wherein one or more amino acids have been deleted, added or replaced by other amino acids, without substantially reducing the enzymatic action of the polypeptide.
 2. DNA sequence according to claim 1, with the amino acid sequence shown in SEQ ID NO:
 1. 3. DNA sequences which code for a polypeptide with the amino acid sequence shown in SEQ ID NO: 14 or for an analogue or derivative of the polypeptide according to SEQ ID NO: 14 wherein one or more amino acids have been deleted, added or replaced by other amino acids, without substantially reducing the enzymatic action of the polypeptide.
 4. DNA sequence according to claim 3, with the amino acid sequence shown in SEQ ID NO:
 9. 5. DNA sequence according to one of claims 1 to 4, characterized in that it also has functional regulation signals, in particular promoters, operators, enhancers and ribosomal binding sites.
 6. DNA sequence with the following part sequences i) promoter which is active in viruses, eukaryotes and prokaryotes and ensures the formation of an RNA in the envisaged target tissue or the target cells, ii) DNA sequence which codes for a polypeptide with the amino acid sequence shown in SEQ ID NO: 5 or 14 or for an analogue or derivative of the polypeptide according to SEQ ID NO: 5 or 14, iii) 3′-nontranslated sequence which leads to the addition of poly-A radicals on to the 3′-end of the RNA in viruses, eukaryotes and prokaryotes.
 7. Expression vector containing one or more DNA sequences according to one of claims 1 to
 4. 8. Protein which participates in the 1-deoxy-D-xylulose 5-phosphate metabolic pathway and a) is coded by the DNA sequence SEQ ID NO: 1 or 9 or b) is coded by DNA sequences which hybridize with the DNA sequences SEQ ID NO: 1 or 9 or fragments of these DNA sequences in the DNA region which codes for the mature protein or c) is coded by DNA sequences which would hybridize with the sequences defined in b) without degeneration of the genetic code and code for a polypeptide with a corresponding amino acid sequence.
 9. Protein according to claim 8, which has the amino acid sequences SEQ ID NO: 5 or
 14. 10. Plant cells containing DNA sequences according to one of claims 1 to
 4. 11. Transformed plant cells and transgenic plants regenerated from these containing DNA sequences according to one of claims 1 to
 4. 12. Transgenic viruses, eukaryotes and prokaryotes with isoprenoid expression, characterized in that they contain a DNA sequence according to one of claims 1 to
 4. 13. Use of a DNA sequence according to one of claims 1 to 4 for determination of the enzymatic activity of the LytB and YfgB protein.
 14. Use of a DNA sequence according to one of claims 1 to 4 for modifying, in particular increasing, the isoprenoid content in viruses and eukaryotic and prokaryotic cells.
 15. Use of DNA sequences according to one of claims 1 to 4 for identification of substances which have an inhibiting action on the LytB and YfgB protein.
 16. Process for isolation of a protein according to claim 8, characterized in that culture supernatants of parasites or of broken-down parasites are purified via chromatographic and electrophoretic techniques.
 17. Process for isolation of a protein according to claim 8, characterized in that it is the product of a viral, prokaryotic or eukaryotic expression of an exogenous DNA.
 18. Method for determination of the enzymatic activity of the LytB and YfgB protein, characterized in that the change in the concentration of the substrates, co-substrates and products is determined.
 19. Process for the production of transgenic viruses, eukaryotes and prokaryotes with isoprenoid expression, characterized in that a DNA sequence according to claim 4 or 5 is transferred and incorporated into the genome of viruses and eukaryotic and prokaryotic cells, with or without the use of a plasmid.
 20. Method for screening a compound, wherein the method comprises: a) provision of a host cell which contains a recombinant expression vector, wherein the vector has at least part of the oligonucleotide sequence according to SEQ ID NO: 1 or SEQ ID NO: 9 or variants or analogues of this, and in addition a compound which is presumed to have an antimycotic, antibiotic, antiparasitic or antiviral action in humans and animals, b) bringing the microorganism into contact with the compound and c) determination of the antimycotic, antibiotic, antiparasitic or antiviral activity of the compound.
 21. Method for screening a compound, wherein the method comprises: a) provision of a host cell which contains a recombinant expression vector, wherein the vector has at least part of the oligonucleotide sequence according to SEQ ID NO: 1 or SEQ ID NO: 9 or variants or analogues of this, and in addition a compound which is presumed to have an antimycotic, antibiotic, antiparasitic or antiviral action in humans and animals, b) bringing the microorganism into contact with the compound and c) determination of the bactericidal, fungicidal or herbicidal activity of the compound. 